FOSFOROMETER— 510(k) K863072

Substantially Equivalent

J. D. Assoc.

FDA 510(k) clearance K863072 for FOSFOROMETER, Substantially Equivalent on 1986-09-09. Applicant: J. D. Assoc.. Device class: 1.

Clearance details

Applicant: J. D. Assoc.
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1986-08-12
Decision date: 1986-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montclair, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CEO

K100263 — ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTS2011-05-06
K072141 — S40 CLINICAL ANALYZER, S TEST IP, S TEST UA2008-06-24
K041643 — SYNCHRON SYSTEMS PHOSPHORUS (PHS) REAGENT2004-08-18
K030015 — ATAC PAK PHOSPHORUS REAGENT2003-03-07
K022312 — PICCOLO PHOSPHORUS TEST SYSTEM2002-09-05

More clearances from J. D. Assoc.

Data sourced from openFDA. This site is unofficial and independent of the FDA.